Canonical Allele Identifier: CA1905817645

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118422C= , CM000672.2:g.43118422C=	GRCh38
NC_000010.10:g.43613870C= , CM000672.1:g.43613870C=	GRCh37
NC_000010.9:g.42933876C=	NCBI36
NG_007489.1:g.46354C= , LRG_518:g.46354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1938C=	ENSP00000480088.2:p.Val646=
ENST00000683007.1:n.1908C=
ENST00000683872.1:n.1899C=
ENST00000340058.6:c.2334C=	ENSP00000344798.4:p.Val778=
ENST00000355710.8:c.2334C= MANE Select	ENSP00000347942.3:p.Val778=
ENST00000671844.1:c.*928C=	ENSP00000500541.1:n.*928C=
ENST00000672389.1:c.*928C=	ENSP00000500252.1:n.*928C=
ENST00000340058.5:c.2334C=	ENSP00000344798.4:p.Val778=
ENST00000355710.7:c.2334C=	ENSP00000347942.3:p.Val778=
ENST00000615310.4:c.1290-1280C=	ENSP00000480088.1:n.1290-1280C=
NM_020630.4:c.2334C= , LRG_518t2:c.2334C=	NP_065681.1:p.Val778=
NM_020975.4:c.2334C= , LRG_518t1:c.2334C=	NP_066124.1:p.Val778=
XM_011540027.1:c.2334C=	XP_011538329.1:p.Val778=
NM_001355216.1:c.1572C=	NP_001342145.1:p.Val524=
NM_020630.5:c.2334C=	NP_065681.1:p.Val778=
NM_020975.5:c.2334C=	NP_066124.1:p.Val778=
NM_020975.6:c.2334C= MANE Select	NP_066124.1:p.Val778=
NM_020630.6:c.2334C=	NP_065681.1:p.Val778=